State Key Laboratory of Microbial Resources, Institute of Microbiology, Chinese Academy of Sciences , Beijing, PR China.
College of Life Sciences, University of Chinese Academy of Sciences , Beijing, PR China.
RNA Biol. 2020 Oct;17(10):1427-1441. doi: 10.1080/15476286.2020.1771946. Epub 2020 Jun 19.
The ribosomal RNA (rRNA) genes are generally organized as an operon and cotranscribed into a polycistronic precursor; therefore, processing and maturation of pre-rRNAs are essential for ribosome biogenesis. However, rRNA maturation pathways of archaea, particularly of methanoarchaea, are scarcely known. Here, we thoroughly elucidated the maturation pathway of the rRNA operon (16S-tRNA-23S-tRNA-5S) in , one representative of methanoarchaea. Enzymatic assay demonstrated that EndA, a tRNA splicing endoribonuclease, cleaved bulge-helix-bulge (BHB) motifs buried in the processing stems of pre-16S and pre-23S rRNAs. Northern blot and quantitative PCR detected splicing-coupled circularization of pre-16S and pre-23S rRNAs, which accounted for 2% and 12% of the corresponding rRNAs, respectively. Importantly, endoribonuclease Nob1 was determined to linearize circular pre-16S rRNA at the mature 3' end so to expose the anti-Shine-Dalgarno sequence, while circular pre-23S rRNA was linearized at the mature 5' end by an unknown endoribonuclease. The resultant 5' and 3' extension in linearized pre-16S and pre-23S rRNAs were finally matured through 5'-3' and 3'-5' exoribonucleolytic trimming, respectively. Additionally, a novel processing pathway of endoribonucleolysis coupled with exoribonucleolysis was identified for the pre-5S rRNA maturation in this methanogen, which could be also conserved in most methanogenic euryarchaea. Based on evaluating the phylogenetic conservation of the key elements that are involved in circularization and linearization of pre-rRNA maturation, we predict that the rRNA maturation mode revealed here could be prevalent among archaea.
核糖体 RNA (rRNA) 基因通常作为一个操纵子组织,并共同转录为多顺反子前体;因此,前 rRNA 的加工和成熟对于核糖体的生物发生是必不可少的。然而,古菌,特别是产甲烷古菌的 rRNA 成熟途径知之甚少。在这里,我们彻底阐明了 ,一种产甲烷古菌的代表,rRNA 操纵子(16S-tRNA-23S-tRNA-5S)的成熟途径。酶促测定表明,tRNA 剪接内切核酶 EndA 切割埋藏在 pre-16S 和 pre-23S rRNAs 加工茎中的凸起-螺旋-凸起 (BHB) 模体。Northern blot 和定量 PCR 检测到 pre-16S 和 pre-23S rRNAs 的剪接偶联环化,分别占相应 rRNAs 的 2%和 12%。重要的是,内核酸酶 Nob1 被确定在线性化环状 pre-16S rRNA 的成熟 3' 端,从而暴露反 Shine-Dalgarno 序列,而环状 pre-23S rRNA 在成熟 5' 端被未知的内核酸酶线性化。线性化的 pre-16S 和 pre-23S rRNAs 中的 5' 和 3' 延伸最终通过 5'-3' 和 3'-5' 外切核酶修剪分别成熟。此外,在这种产甲烷菌中,还鉴定了一种新的内含子切割与外切核酶切割相结合的前 5S rRNA 成熟加工途径,该途径在大多数产甲烷古菌中也可能保守。通过评估参与 pre-rRNA 成熟的环状和线性化的关键元件的系统发育保守性,我们预测这里揭示的 rRNA 成熟模式可能在古菌中普遍存在。